FDA UDI
In Commercial Distribution
🇺🇸 United States
GluLink
DI: 06975640490013
·
Model: /
·
HeYuan FandDing Medical Co Ltd
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1
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Basic Information
- Brand Name
- GluLink
- Primary DI
- 06975640490013
- Version / Model
- /
- Company Name
- HeYuan FandDing Medical Co Ltd
- Labeler DUNS
- 711353062
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2022-11-17
- Public Version
- 1
- Public Version Date
- 2022-11-25
- Public Version Status
- New
- Public Device Record Key
- ea15c2f2-9374-49de-8715-20565ea3936b
Device Characteristics
- Single Use
- No
- Prescription Use (Rx)
- No
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- Yes
- Has Serial Number
- Yes
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- Yes
- Has Expiration Date
- No
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| OUG | Medical Device Data System | General Hospital | 880.6310 | 1 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 64412 | Rapid test/self-testing data interpretive/transfer/validation software IVD | A software program intended to be used by a healthcare professional or patient to capture, interpret, transfer, and/or validate the results of data from an in vitro diagnostic rapid test/self-test [e.g., SARS-CoV-2 antigen/antibody self-test, influenza virus immunochromatographic rapid test (ICT), glucose rapid test] using a mobile device (e.g., smartphone, tablet). The results are transmitted to an Internet-based platform or a centralized database for assessment by a healthcare professional and/or for clinical research applications. Data may be reviewed by the patient and clinician, or not made available to the patient. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 06975640490006 | GS1 | 1 | In Commercial Distribution | ||
| Primary | 06975640490013 | GS1 |